ClinVar Miner

List of variants in gene POLG reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP
NM_002693.2(POLG):c.-160+6C>T rs886051526
NM_002693.2(POLG):c.-170T>A rs796052915
NM_002693.2(POLG):c.-241C>T rs886051527
NM_002693.2(POLG):c.-67A>G rs553331485
NM_002693.2(POLG):c.-80C>T rs3087378
NM_002693.2(POLG):c.1066C>T (p.Leu356=) rs371431444
NM_002693.2(POLG):c.1084C>G (p.Leu362Val) rs763248358
NM_002693.2(POLG):c.1156C>T (p.Arg386Cys) rs199759055
NM_002693.2(POLG):c.1170+6G>A rs749250690
NM_002693.2(POLG):c.1171-11C>T rs886051525
NM_002693.2(POLG):c.1311C>T (p.Val437=) rs62640035
NM_002693.2(POLG):c.1327C>T (p.Arg443Cys) rs747485523
NM_002693.2(POLG):c.1356T>C (p.Tyr452=) rs3176179
NM_002693.2(POLG):c.1386G>A (p.Ser462=) rs62640034
NM_002693.2(POLG):c.1402A>G (p.Asn468Asp) rs145843073
NM_002693.2(POLG):c.1498G>A (p.Ala500Thr) rs745506700
NM_002693.2(POLG):c.1585+11T>C rs201566815
NM_002693.2(POLG):c.1599C>G (p.Cys533Trp) rs754246294
NM_002693.2(POLG):c.1626T>C (p.Asp542=) rs376576519
NM_002693.2(POLG):c.1629C>T (p.Val543=) rs56349446
NM_002693.2(POLG):c.1743C>T (p.Asp581=) rs140743000
NM_002693.2(POLG):c.1886A>C (p.Asp629Ala) rs1039182766
NM_002693.2(POLG):c.1887C>T (p.Asp629=) rs886051524
NM_002693.2(POLG):c.1898A>C (p.Lys633Thr) rs568913937
NM_002693.2(POLG):c.1902G>T (p.Leu634=) rs886051523
NM_002693.2(POLG):c.1905G>A (p.Pro635=) rs550592814
NM_002693.2(POLG):c.2021G>A (p.Gly674Asp) rs200257554
NM_002693.2(POLG):c.2028G>A (p.Ala676=) rs373550219
NM_002693.2(POLG):c.2071-14T>G rs150088708
NM_002693.2(POLG):c.2109C>T (p.Ala703=) rs2307429
NM_002693.2(POLG):c.2157+11C>T rs56411159
NM_002693.2(POLG):c.2157+15G>A rs766521182
NM_002693.2(POLG):c.2207A>G (p.Asn736Ser) rs138457939
NM_002693.2(POLG):c.2218A>G (p.Asn740Asp) rs78347903
NM_002693.2(POLG):c.2265+1G>C rs796052884
NM_002693.2(POLG):c.2266-11G>C rs747154432
NM_002693.2(POLG):c.2279G>A (p.Cys760Tyr) rs752878861
NM_002693.2(POLG):c.2354G>A (p.Gly785Asp) rs149058889
NM_002693.2(POLG):c.2481-10A>C rs555280530
NM_002693.2(POLG):c.2481-7C>T rs2307448
NM_002693.2(POLG):c.2541C>T (p.Ala847=) rs143810171
NM_002693.2(POLG):c.2601T>C (p.Pro867=) rs201749977
NM_002693.2(POLG):c.2642C>T (p.Pro881Leu) rs375935084
NM_002693.2(POLG):c.264C>T (p.Phe88=) rs144439703
NM_002693.2(POLG):c.2724C>T (p.Ala908=) rs377390914
NM_002693.2(POLG):c.2735-7C>G rs200372494
NM_002693.2(POLG):c.2830G>A (p.Glu944Lys) rs768653086
NM_002693.2(POLG):c.2853C>T (p.Tyr951=) rs41546712
NM_002693.2(POLG):c.2939A>C (p.Glu980Ala) rs754202777
NM_002693.2(POLG):c.3076C>T (p.Arg1026Cys) rs760043525
NM_002693.2(POLG):c.3098C>T (p.Ala1033Val) rs551708243
NM_002693.2(POLG):c.3131T>C (p.Val1044Ala) rs150233690
NM_002693.2(POLG):c.3176A>G (p.Asn1059Ser) rs201192905
NM_002693.2(POLG):c.3197C>T (p.Thr1066Met) rs750794449
NM_002693.2(POLG):c.3198G>A (p.Thr1066=) rs61752780
NM_002693.2(POLG):c.3229T>G (p.Cys1077Gly) rs1567185468
NM_002693.2(POLG):c.3239G>C (p.Ser1080Thr) rs779956099
NM_002693.2(POLG):c.3273+6T>A rs886051522
NM_002693.2(POLG):c.32G>A rs765472726
NM_002693.2(POLG):c.3334A>T (p.Met1112Leu) rs767168260
NM_002693.2(POLG):c.3424C>T (p.Arg1142Trp) rs2307442
NM_002693.2(POLG):c.3482+6C>T rs55779802
NM_002693.2(POLG):c.3549C>T (p.Val1183=) rs777231247
NM_002693.2(POLG):c.391T>C (p.Tyr131His) rs562847013
NM_002693.2(POLG):c.452T>C (p.Leu151Pro) rs749018627
NM_002693.2(POLG):c.578G>A (p.Arg193Gln) rs3176162
NM_002693.2(POLG):c.678G>C (p.Gln226His) rs147282197
NM_002693.2(POLG):c.729C>A (p.Asp243Glu) rs757917194
NM_002693.2(POLG):c.798G>T (p.Val266=) rs143631183
NM_002693.2(POLG):c.803G>C (p.Gly268Ala) rs61752784
NM_002693.2(POLG):c.87C>T (p.Ser29=) rs587781116
NM_002693.2(POLG):c.970C>T (p.Pro324Ser) rs2307437
NM_002693.3(POLG):c.-262C>T
NM_002693.3(POLG):c.1057G>A (p.Val353Ile)
NM_002693.3(POLG):c.1062C>T (p.Asn354=)
NM_002693.3(POLG):c.109G>A (p.Asp37Asn)
NM_002693.3(POLG):c.1439A>G (p.Lys480Arg)
NM_002693.3(POLG):c.1910G>A (p.Gly637Asp)
NM_002693.3(POLG):c.2040G>A (p.Leu680=)
NM_002693.3(POLG):c.2159C>G (p.Thr720Ser)
NM_002693.3(POLG):c.2988G>A (p.Arg996=)
NM_002693.3(POLG):c.3120G>C (p.Lys1040Asn)
NM_002693.3(POLG):c.3151G>T (p.Gly1051Trp)
NM_002693.3(POLG):c.3561G>T (p.Arg1187=)
NM_002693.3(POLG):c.494A>G (p.Lys165Arg)
NM_002693.3(POLG):c.830A>T (p.His277Leu) rs138929605

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